MY125533A - Heterocyclic dihydropyrimidine compounds - Google Patents
Heterocyclic dihydropyrimidine compoundsInfo
- Publication number
- MY125533A MY125533A MYPI20005460A MYPI20005460A MY125533A MY 125533 A MY125533 A MY 125533A MY PI20005460 A MYPI20005460 A MY PI20005460A MY PI20005460 A MYPI20005460 A MY PI20005460A MY 125533 A MY125533 A MY 125533A
- Authority
- MY
- Malaysia
- Prior art keywords
- compounds
- inhibitors
- ikur
- dihydropyrimidine compounds
- heterocyclic dihydropyrimidine
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A—HUMAN NECESSITIES
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Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
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- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
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- Neurosurgery (AREA)
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- Virology (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Pulmonology (AREA)
- Heart & Thoracic Surgery (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Molecular Biology (AREA)
- Hospice & Palliative Care (AREA)
- Urology & Nephrology (AREA)
- Biotechnology (AREA)
Abstract
NOVEL HETEROCYCLIC DIHYDROPYRIMIDINE COMPOUNDS USEFUL AS INHIBITORS OF POTASSIUM CHANNEL FUNCTION (ESPECIALLY INHIBITORS OF THE Kv1 SUBFAMILY OF VOLTAGE GATED K⁺ CHANNELS, ESPECIALLY INHIBITORS Kv1.5 WHICH HAS BEEN LINKED TO THE ULTRA-RAPIDLY ACTIVATING DELAYED RECTIFIER K+ CURRENT Ikur), METHODS OF USING SUCH COMPOUNDS IN THE PREVENTION AND TREATMENT OF ARRHYTHMIA AND Ikur-ASSOCIATED CONDITIONS, AND PHARMACEUTICAL COMPOSITIONS CONTAINING SUCH COMPOUNDS.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US16909199P | 1999-12-06 | 1999-12-06 | |
US23603700P | 2000-09-28 | 2000-09-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
MY125533A true MY125533A (en) | 2006-08-30 |
Family
ID=26864749
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MYPI20005460A MY125533A (en) | 1999-12-06 | 2000-11-21 | Heterocyclic dihydropyrimidine compounds |
Country Status (25)
Country | Link |
---|---|
US (3) | US6706720B2 (en) |
EP (1) | EP1237891B1 (en) |
JP (1) | JP2004507442A (en) |
KR (1) | KR20020060255A (en) |
CN (1) | CN1407985A (en) |
AR (1) | AR029457A1 (en) |
AT (1) | ATE526329T1 (en) |
AU (1) | AU781862B2 (en) |
BR (1) | BR0016166A (en) |
CA (1) | CA2393809C (en) |
CO (1) | CO5570109A1 (en) |
CZ (1) | CZ20021949A3 (en) |
HK (1) | HK1048808A1 (en) |
HU (1) | HUP0301834A3 (en) |
IL (2) | IL149473A0 (en) |
MX (1) | MXPA02005533A (en) |
MY (1) | MY125533A (en) |
NO (1) | NO323588B1 (en) |
NZ (1) | NZ518663A (en) |
PE (1) | PE20011029A1 (en) |
PL (1) | PL364926A1 (en) |
RU (1) | RU2296766C2 (en) |
TW (1) | TWI291465B (en) |
UY (1) | UY26472A1 (en) |
WO (1) | WO2001040231A1 (en) |
Families Citing this family (155)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9901691D0 (en) | 1999-01-26 | 1999-03-17 | Cerebrus Ltd | Chemical compounds |
MY125533A (en) * | 1999-12-06 | 2006-08-30 | Bristol Myers Squibb Co | Heterocyclic dihydropyrimidine compounds |
GEP20053688B (en) * | 2000-06-30 | 2005-12-12 | Wyeth Corp | Substituted-Triazolopyrimidines as Anticancer Agents |
CZ297570B6 (en) * | 2000-12-25 | 2007-02-07 | Sankyo Company, Limited | Pharmaceutical formulations containing 2-acetoxypyridine derivative and aspirin |
TWI243164B (en) | 2001-02-13 | 2005-11-11 | Aventis Pharma Gmbh | Acylated indanyl amines and their use as pharmaceuticals |
KR20030096348A (en) * | 2001-05-05 | 2003-12-24 | 스미스클라인비이참피이엘시이 | N-aroyl cyclic amines |
EP1435955A2 (en) * | 2001-05-05 | 2004-07-14 | SmithKline Beecham P.L.C. | N-aroyl cyclic amine derivatives as orexin receptor antagonists |
US7139344B2 (en) * | 2001-05-16 | 2006-11-21 | Lexmark International, Inc. | Method and apparatus for effecting synchronous pulse generation for use in variable speed serial communications |
GB0115862D0 (en) * | 2001-06-28 | 2001-08-22 | Smithkline Beecham Plc | Compounds |
JP4399256B2 (en) * | 2001-06-28 | 2010-01-13 | スミスクライン ビーチャム ピー エル シー | N-aroyl cyclic amine derivatives as orexin receptor antagonists |
BRPI0212726B8 (en) | 2001-09-21 | 2021-05-25 | Bristol Myers Squibb Co | compounds containing lactams, and derivatives thereof, pharmaceutical composition comprising them and their uses |
WO2003037900A2 (en) * | 2001-11-01 | 2003-05-08 | Icagen, Inc. | Pyrazolopyrimidines |
US7435824B2 (en) | 2002-04-19 | 2008-10-14 | Bristol-Myers Squibb Company | Prodrugs of potassium channel inhibitors |
CA2487211C (en) * | 2002-06-04 | 2010-09-14 | Neogenesis Pharmaceuticals, Inc. | Pyrazolo(1,5a) pyrimidine compounds as antiviral agents |
WO2004071440A2 (en) | 2003-02-06 | 2004-08-26 | Bristol-Myers Squibb Company | Thiazolyl-based compounds useful as kinase inhibitors |
US6846836B2 (en) | 2003-04-18 | 2005-01-25 | Bristol-Myers Squibb Company | N-substituted phenylurea inhibitors of mitochondrial F1F0 ATP hydrolase |
WO2004098518A2 (en) | 2003-05-01 | 2004-11-18 | Bristol-Myers Squibb Company | Pyrazole-amide compounds useful as kinase inhibitors |
GB0315950D0 (en) | 2003-06-11 | 2003-08-13 | Xention Discovery Ltd | Compounds |
US20050187278A1 (en) * | 2003-08-28 | 2005-08-25 | Pharmacia Corporation | Treatment or prevention of vascular disorders with Cox-2 inhibitors in combination with cyclic AMP-specific phosphodiesterase inhibitors |
WO2005044793A2 (en) * | 2003-10-31 | 2005-05-19 | Takeda Pharmaceutical Company Limited | Nitrogen-containing fused heterocyclic compounds |
US7550499B2 (en) | 2004-05-12 | 2009-06-23 | Bristol-Myers Squibb Company | Urea antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
PL1750862T3 (en) | 2004-06-04 | 2011-06-30 | Teva Pharma | Pharmaceutical composition containing irbesartan |
GB0412986D0 (en) | 2004-06-10 | 2004-07-14 | Xention Discovery Ltd | Compounds |
US7253167B2 (en) * | 2004-06-30 | 2007-08-07 | Bristol-Myers Squibb Company | Tricyclic-heteroaryl compounds useful as kinase inhibitors |
US7429611B2 (en) * | 2004-09-23 | 2008-09-30 | Bristol-Myers Squibb Company | Indole inhibitors of 15-lipoxygenase |
US7754755B2 (en) * | 2004-09-23 | 2010-07-13 | Bristol-Myers Squibb Company | Inhibitors of 15-lipoxygenase |
US20060128726A1 (en) * | 2004-11-24 | 2006-06-15 | Xuebao Wang | Process for preparing novel crystalline forms of (2S)-1-[[(7R)-7-(3,4-dichlorophenyl)-4,7-dihydro-5-methylpyrazolo[1,5]pyrimidine-6-yl]carbonyl]-2-(4-fluorophenyl)pyrrolidine, novel stable forms produced therein and formulations |
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